荧光寿命成像显微镜
荧光
显微镜
条纹照相机
荧光显微镜
分辨率(逻辑)
显微镜
费斯特共振能量转移
条纹
光学
图像分辨率
材料科学
荧光互相关光谱
时间分辨率
核磁共振
荧光光谱法
物理
人工智能
计算机科学
激光器
作者
Masanobu Fujiwara,William Cieslik
出处
期刊:Methods in Enzymology
日期:2006-01-01
被引量:5
标识
DOI:10.1016/s0076-6879(06)14033-1
摘要
A newly developed fluorescence lifetime imaging microscopy (FLIM) system has combined the high-temporal resolution of a streak camera with the high-spatial resolution of a microscope to obtain a two-dimensional distribution of fluorescence lifetimes within living cells. The temporal resolution is as short as 20 ps. The effective field of view is 48 x 45 mum with 0.2 mum resolution using a 60x water immersion objective. Image acquisition time is as short as 3 s per image. Measured and published values of lifetime for standard fluophores are shown with good agreement. Examples of FLIM and fluorescence resonance energy transfer images are presented.
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